Gene Locus : human-TG
Mode of mutation : Natural mutant
Disease : Goiter, familial with hypothyroidism, autosomal recessive
Summary : Congenital goiter with hypothyroidism Natural mutation congenital hypothyroidism with goitre Hishinuma_2006_J.Clin.Endocrinol.Metab_91_3100
AAA Change :
Allelic Variant :
Risk Factor :
Inhibitor :
Structure :
Disease by interaction :
Interact Gene Locus :
Xenobiotic sensitivity :
Modification :
Torpedo_number : No torpedo number
Kinetic Parameter : No kinetic parameter
News : No news
Comment :
p.C1077R Cys1077Arg c.3229T>C (p.C1058R Cys1058Arg without 19-amino-acid signal peptide)
Title : Haplotype analysis reveals founder effects of thyroglobulin gene mutations C1058R and C1977S in Japan - Hishinuma_2006_J.Clin.Endocrinol.Metab_91_3100 |
Author(s) : Hishinuma A , Fukata S , Nishiyama S , Nishi Y , Oh-Ishi M , Murata Y , Ohyama Y , Matsuura N , Kasai K , Harada S , Kitanaka S , Takamatsu J , Kiwaki K , Ohye H , Uruno T , Tomoda C , Tajima T , Kuma K , Miyauchi A , Ieiri T |
Ref : J Clinical Endocrinology Metab , 91 :3100 , 2006 |
Abstract : |
PubMedSearch : Hishinuma_2006_J.Clin.Endocrinol.Metab_91_3100 |
PubMedID: 16720658 |
Title : High incidence of thyroid cancer in long-standing goiters with thyroglobulin mutations - Hishinuma_2005_Thyroid_15_1079 |
Author(s) : Hishinuma A , Fukata S , Kakudo K , Murata Y , Ieiri T |
Ref : Thyroid , 15 :1079 , 2005 |
Abstract : |
PubMedSearch : Hishinuma_2005_Thyroid_15_1079 |
PubMedID: 16187918 |